Drug intelligence / Profile preview

visilizumab

Development stage
Phase 3
Lead developer
PDL BioPharma
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Recombinant Proteins and Enzymes
Administration
Intravenous
01

Overview

Visilizumab is a humanized, non-Fc receptor (FcR)-binding IgG2 monoclonal antibody directed against the CD3 receptor on activated T cells. Developed by PDL BioPharma, it was investigated as an immunosuppressive agent for immune-mediated diseases such as ulcerative colitis and Crohn's disease. The drug binds to the invariant CD3 epsilon subunit of the T-cell receptor complex on activated T cells, inducing apoptosis predominantly in mucosal CD4+ T lymphocytes via caspase 3 and 8 activation, without affecting resting or peripheral blood T cells. This mechanism aims to rapidly eliminate pathogenic T cells in inflamed tissues while minimizing cytokine release toxicity due to its engineered Fc region that prevents FcR binding. Despite initial promise, clinical development was discontinued after Phase II/III trials due to insufficient efficacy and safety compared with other therapies[1][4][5][6][8].

Brand names
Nuvion
Other names
Monoclonal antibody anti-CD3 humanisedVisiluzumab
02

Targets

CD3 (T-cell surface glycoprotein CD3)

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